Three chemokines, Mig, IP-10, and I-TAC, are expressed highly, in the epide
rmis. We examined the expression of the receptor for these chemokines, CXCR
3, in cutaneous T-cell lymphoma. We compared CXCR3 expression with that of
cutaneous lymphocyte antigen (CLA) and the activation marker CD30. CXCR3 wa
s expressed by at least a subset of tumor lymphocytes in all 25 cases of lo
w-grade mycosis fungoides IMF), with most cells positive in 20 cases. In pr
ogressed or transformed MF, CXCR3 expression was noted in 5 of 22 cases. In
4 of 5 MF cases with sequential biopsy specimens, large cell transformatio
n was accompanied by loss of CXCR3 expression. In contrast, CLA was express
ed in 35 of 42 MF cases with no significant differences in expression level
between low-grade and transformed cases. In other lymphomas, CXCR3 was exp
ressed in 4 of 4 cases of lymphomatoid papulosis, 3 of 4 cases of CD8+ cuta
neous T-cell lymphoma, and 3 of 6 cases of systemic T-cell lymphoma in skin
, but not in 10 cases of cutaneous anaplastic large cell lymphoma. CXCR3 ex
pression was associated with epidermotropic T-cell tumors but was largely a
bsent in dermal-based tumors. This phenotypic change likely influences the
loss of epidermal localization.